Author
Hamad bin Khalifa UniversityORCID 0000-0001-5916-5983Unclaimed ORCID profile · follow to get notified of new preprints
Mutual co-authors in cluster
6 papers
Recent·Most cited
Nayra M. Al‐Thani, Shaza B. Zaghlool, Salman M. Toor…·Omar Albagha
The paper subtypes Type 2 Diabetes in a Middle Eastern cohort, identifies sex differences, and highlights the need for personalized treatment strategies based on subtype-specific risks.
Umm‐Kulthum Ismail Umlai, Salman M. Toor, Yasser A. Al-Sarraj…·Omar Albagha
This study identifies a novel SLC2A9 variant associated with LDL-C levels in Qatar's Middle Eastern population and evaluates polygenic scores across ancestries.
Jamil Alenbawi, Yasser A. Al-Sarraj, Umm‐Kulthum Ismail Umlai…·Omar Albagha
This paper identifies novel genetic loci associated with serum campesterol levels through GWAS and meta-analysis in a MENA population, and develops a polygenic risk score for sitosterolemia.
Nick R. G. Shrine, Abril G. Izquierdo, Jing Chen…·Data Management and Computing Infrastructure group
This study performs a multi-ancestry GWAS on lung function and COPD, identifying 559 genes and 29 pathways, and showing genetic risk scores are associated with COPD across ancestries.
Hamdi Mbarek, Geethanjali Devadoss Gandhi, Senthil Selvaraj…·Asma Al-Thani
The Qatar Genome Program sequenced 6,045 individuals, identifying 88 million variants, including novel ones, and revealed genetic structure and disease-related markers in the Qatari population.
Ilhame Diboun, Sachin Wani, Stuart H. Ralston, Omar Albagha
This study identifies differentially methylated loci in blood samples of Paget's disease of bone patients, showing their potential as diagnostic markers.